State

US Virgin Islands product recalls

73,817 recalls have nationwide distribution and so reach US Virgin Islands. 178 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total: 178
Critical: 12
Severe: 39
Most recent: 2026-10-21

Of the 178 recalls naming US Virgin Islands we have scored against our rubric, 12 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 39 (22%) are Severe.

Which agencies issued them

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48976–49000 of 73995

HighFDA (Devices)·Z-1583-2016·2016-05-04
Mako Surgical Recalls RESTORIS PST RIO Offset Shell Impactor
Mako Surgical Corporation is recalling 96 units of the RESTORIS PST RIO Offset Shell Impactor due to a potential disassociation of the orientation pin.
Product
RESTORIS PST RIO Offset Shell Impactor For use by orthopedic surgeons specifically for the purpose of positioning and implanting acetabular cup components during Total Hip Arthroplasty (THA) surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1584-2016·2016-05-04
Research Instruments Recalls Integra 3 Micromanipulators Due to Faulty Power Cable
Research Instruments Ltd is recalling 380 Integra 3 micromanipulators because they were fitted with a potentially faulty power supply cable.
Product
Integra 3; Model Numbers: 6-54-100, 6-54-110, 6-54-150, 6-54-160 Product Usage: The Rl TDU500 Micromanipulator for Assisted Reproduction is used to accurately position microtools under a microscope for the techniques of Assisted Reproduction. The Rl Integra is a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1554-2016·2016-05-04
Horiba Recalls ABX Pentra 400 and C400 Clinical Chemistry Analyzers
Horiba Instruments is recalling ABX Pentra 400 and Pentra C400 analyzers due to malfunctions triggered by specific system alarms.
Product
Pentra C400 (version 1.1.2 or lower) The ABX PENTRA 400 and 400C are discrete photometric bench top chemistry analyzers for clinical use. The device is intended to duplicate manual analytical procedures by performing various steps such as pipetting, mixing, heating and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1559-2016·2016-05-04
Becton Dickinson Recalls Listeria-Contaminated Trypticase Soy Agar Plates
Becton Dickinson is recalling Trypticase Soy Agar and MacConkey II Agar plates contaminated with Listeria monocytogenes. The non-sterile media are used for growing and detecting bacteria.
Product
Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) // MacConkey II Agar Cat. Number 221291, Lot Number 6034889, Exp. Date : April 20, 2016 Product is sold in cartons of 100 plates each. Product Usage: Trypticase Soy Agar with 5% Sheep Blood is used for the growth of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1553-2016·2016-05-04
Horiba Recalls ABX Pentra 400 Analyzers Due to Malfunctions
Horiba Instruments is recalling ABX Pentra 400 and Pentra C400 analyzers because they malfunction when specific alarms appear on the system.
Product
ABX Pentra 400 (version 5.0.8 or lower) The ABX PENTRA 400 and 400C are discrete photometric bench top chemistry analyzers for clinical use. The device is intended to duplicate manual analytical procedures by performing various steps such as pipetting, mixing, heating and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1561-2016·2016-05-04
Elekta Radionuclide Radiation Therapy System Recalled for Frame Adapter Latch Defect
Elekta is recalling 217 Radionuclide Radiation Therapy Systems because frame adapter latches can lock without proper pin insertion, potentially compromising treatment accuracy.
Product
Radionuclide Radiation Therapy System Product The product is a teletherapy device intended for stereotactic irradiation of head structures ranging from very small target sizes of a few millimeters to several centimeters.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V269000·2016-05-04
Auto Truck Recalls IMT Dominator Series III Vehicles Due to Valve Cover Defect
Auto Truck is recalling 2013-2016 IMT Dominator Series III vehicles because a valve bank cover may crack and fall off, creating a road hazard.
Product
AUTO TRUCK — AUTO TRUCK IMT DOMINATOR SERIES III
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1558-2016·2016-05-04
Siemens SOMATOM Force CT Systems Recalled for Image Artifacts
Siemens is recalling 37 SOMATOM Force CT systems because a software error in the Neonate Head protocol may cause image artifacts, potentially leading to misdiagnosis.
Product
SOMATOM Force, Computed Tomography x-ray system intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V268000·2016-05-04
Volvo Recalls 2016 XC90 Vehicles Due to Sunroof Switch Defect
Volvo is recalling 2016 XC90 vehicles because the sunroof switch may be unintentionally pressed, causing the panel to close and increasing the risk of occupant injury.
Product
VOLVO — VOLVO XC90
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1578-2016·2016-05-04
Roche IT3800 Hand-Held Barcode Scanner Recalled for Mis-Identification
Roche Molecular Systems is recalling 6,939 IT3800 hand-held barcode scanners because they mis-identified sample barcodes when used with the COBAS AmpliPrep instrument.
Product
Hand-Held Scanner USB IT3800 For sample identification and tracking when used with various systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1585-2016·2016-05-04
Shimadzu X-Ray Diagnostic Table Recalled for Unintentional Reverse Tilting
Shimadzu Medical Systems is recalling 185 X-Ray Diagnostic Tables (Model YSF-300) due to reports of unintentional movement to reverse tilting.
Product
X-Ray Diagnostic Table, Model No. YSF-300 Use in combination with an X-ray high voltage generator, an X-ray tube unit, an Image intensifier and X-ray television unit, this table is applied for the following X-ray examinations: -X-ray T.V. fluoroscopy -Spot-filming -Bucky…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1568-2016·2016-05-04
Intuitive Surgical Recalls da Vinci Xi Stapler Instruments Due to Motion Risk
Intuitive Surgical is recalling 43 EndoWrist Stapler instruments for the da Vinci Xi system due to a risk of unexpected jaw motion during use.
Product
EndoWrist Stapler 45 and Stapler 30 instruments used on the da Vinci Xi systems (IS4000) with p5 software. General Surgery: The Intuitive Surgical Endoscope Instrument Control System (da Vinci Surgical System, Model IS4000) is intended to assist in the accurate control of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1528-2016·2016-05-04
Corin Trinity Acetabular Shell Recall Due to Packaging Abrasion Risk
Corin USA Limited is recalling 629 Trinity Acetabular Shells used in total hip replacements because the new packaging system may abrade the sterile barrier pouches.
Product
Trinity Acetabular Shell Product Usage Total Hip Replacement.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1125-2016·2016-05-04
Liquid Coffee Inc Recalls Concentrated Coffee Due to Elevated pH Levels
Liquid Coffee Inc is recalling 642 gallons of concentrated coffee because the pH level was elevated above 4.6. The product was distributed nationwide to specific states.
Product
Concentrated coffee packed in 1/2 gallon or 1 gallon hermetically sealed Scholle or Liquibag.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1260-2016·2016-05-04
Family Gourmet White Rice Recalled Due to Live Insects
Family Dollar is recalling Family Gourmet Long Grain Enriched White Rice because live insects were found inside unopened bags.
Product
Family Gourmet Long Grain Enriched White Rice, 32 oz. (2 lb.) plastic bag (SKU: 1218898)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1567-2016·2016-05-04
Boston Scientific Recalls Mislabeled Ultraflex Tracheobronchial Stents
Boston Scientific is recalling four Ultraflex Tracheobronchial stents because 10mm diameter units were mislabeled as 12mm diameter.
Product
Boston Scientific Ultraflex Tracheobronchial Distal Release Stent System 12mm X 30mm Material Number: M00576550 The stent system is a permanently implanted expandable metal stent designed for palliation of tracheobronchial (TB) strictures. The system consists of a flexible…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1575-2016·2016-05-04
Mindray Panorama Patient Monitoring Network Recalled for Date Reversion
Mindray DS USA is recalling Panorama Patient Monitoring Network units that may revert to the year 2000 during Daylight Savings Time.
Product
Panorama Patient Monitoring Network Mindray DS USA The Panorama Patient Monitoring can view recal time, store, print, graph and trend patient clinical and demographic data. The Panoram Patient Monitoring Network can sent independent alarm limits for data send by the bedside…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1564-2016·2016-05-04
Hansen Medical Recalls Magellan Robotic Catheter Accessory Kits
Hansen Medical is recalling eight Magellan Robotic Catheter Accessory Kits because one batch was radiated below the required dose.
Product
Magellan Robotic Catheter Accessory Kits, Model number MACC 50 and MACC80. Cardiology: The Hansen Medical Magellan System is a robotic control system that enables positioning and visualization of a Magellan Catheter and an off-the-shelf guide wire while allowing a physician…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1261-2016·2016-05-04
Family Gourmet Brown Rice Recalled Due to Live Insects
Family Dollar is recalling Family Gourmet Natural Whole Grain Brown Rice because live insects were found in unopened bags.
Product
Family Gourmet Natural Whole Grain Brown Rice, 32 oz. (2 lb.) plastic bag (SKU: 1230394)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1527-2016·2016-05-04
Corin Trinity Acetabular Shell Recalled for Packaging Abrasion Risk
Corin USA Limited is recalling 629 Trinity Acetabular Shell devices used in total hip replacements due to a potential for abrasion of the sterile barrier pouches in the new packaging system.
Product
Trinity Acetabular Shell Product Usage: Total Hip Replacement.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1246-2016·2016-05-04
Bissinger's Milk Chocolate Eggs Recalled for Mislabeling Artificial Vanillin as Vanilla
Karl Bissinger, LLC is recalling Bissinger's Milk Chocolate Eggs because the product contains artificial vanillin but is labeled as containing vanilla.
Product
Bissinger's Milk Chocolate Eggs packaged in 6.5 oz (UPC 846107009382) Item: #11108 or 1 lb. (UPC 846107003458) Item: # 111049 plastic bags. Bissinger's Handcrafted Chocolatier, St. Louis, MO.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1526-2016·2016-05-04
Corin Trinity Acetabular System Recalled for Packaging Abrasion Risk
Corin USA Limited is recalling 629 Trinity Acetabular System devices due to potential abrasion of sterile barrier pouches in the new packaging system.
Product
Trinity Acetabular System Product Usage - Total Hip Replacement.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1566-2016·2016-05-04
Stryker PneumoSure Insufflators Recalled for Flow Rate Drop
Stryker Endoscopy is recalling PneumoSure insufflators because the flow rate drops to zero when connected to a house gas source, suspending insufflation.
Product
PneumoSure XL High Flow Insufflator and PneumoSure High Flow Insufflator; High pressure units (HPU) (40L and 45L). Model Numbers: 620-040-610, 620-040-611, 620-040-613, 620-040-614, 620-040-600, 620-040-601, 620-040-602, 620-040-604, 105-210-684 The Pneumo Sure XL High…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1582-2016·2016-05-04
Teleflex Pleur-evac Chest Drainage System Recalled for Missing Tyvek Bag Label
Teleflex Medical is recalling Pleur-evac Chest Drainage Systems because the Tyvek bag label is missing, preventing identification of material code, lot number, and expiration date.
Product
Pleur-evac Chest Drainage System, Dry Suction/Dry Seal Control, REF A-6000-08LF, Rx Only, Teleflex Medical. Product Usage: Pleur-Evacs are sterile, single-use, chest drainage systems intended for post-operative use
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0834-2016·2016-05-04
SKY Aspirin Chewable Tablets Recalled for Incorrect Outer Carton Labeling
McKesson Packaging Services is recalling SKY Aspirin Chewable Tablets because the outer cartons were incorrectly labeled. The recall addresses a labeling mix-up.
Product
SKY Aspirin Chewable Tablets, 81 mg, Unit Dose 750 tablets (25 x 30) box, OTC, Distributed by: McKesson Packaging Service, Concord, NC 28027, NDC 63739-434-01.
Category
Drug
Distribution
Distributed nationwide